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Vasculopathy in Turner Syndrome

机译:特纳综合征的血管病变

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Dissection or rupture of the aorta accounts for death in 2-8% of women with Turner Syndrome (TS), Dilatation of the root of the aorta, hypertension and bicuspid aortic valve have been reported as predisposing factors for aortic dissection but the underlying pathogenesis of vascular dilation in TS is unknown Recent papers 'have revealed that dilatation of the arterial tree in TS extends beyond the aorta to conduit vessels including the carotid and brachial arteries. The distal extent of this dilation is unknown. This finding of widespread arterial dilation appears to represent an unusual 'vasculopathy' in Turner's syndrome. In trying to understand the pathogenesis of this vasculopathy, several aspects of arterial wall integrity lend themselves to scrutiny. There may be a defect of composition or remodelling of connective tissue, an inflammatory process or abnormal smooth muscle contractility thinking particularly of the nitric oxide pathway. Such processes can be exacerbated other features of TS including oestrogen deficiency, hypertension and accelerated atherosclerosis.
机译:Aorta的解剖或破裂占2-8%患有特变型综合征(TS)的妇女死亡,据报道,主动脉,高血压和双囊主动脉瓣的膨胀是主动脉解剖的概述因素,但是潜在的发病机制TS的血管扩张是未知的近期纸张'揭示了Ts中的动脉树的扩张延伸到主动脉,导管包括颈动脉和肱动脉。这种扩张的远端程度未知。这种普遍的动脉扩张的发现似乎代表了特纳综合征的异常“血管病”。在试图理解这种血管病变的发病机制时,动脉墙诚信的几个方面赋予了仔细审查。可以存在结缔组织的组成或重塑,炎症过程或尤其是一氧化氮途径的异常平滑肌肉收缩力的缺陷。这些过程可以加剧TS的其他特征,包括雌激素缺乏,高血压和加速动脉粥样硬化。

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